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Klippel-Trenaunay-Weber Syndrome

机译:Klippel-Trenaunay-Weber综合征

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摘要

The parents of this 2-year-old boy brought their son for evaluation of swelling of the right leg and excoriation and serosanguineous discharge from the ankle region of 3 days' duration. The child had had a hemangioma of the right ankle since birth. Subsequently, there was gradual spread of the lesion along the leg to the buttocks.This patient had Klippel-Trenaunay-Weber syndrome with secondary celluli-tis of the leg.Hemangiomas are common in infancy and are often benign. Klippel-Trenaunay-Weber syndrome is characterized by the triad of capillary and venous malformations, venous varicos-ity, and hyperplasia of soft tissue in the affected area. Parkes Weber syndrome is diagnosed when this triad is accompanied by an arteriovenous fistula.
机译:这个2岁男孩的父母带了他们的儿子,进行了3​​天的评估,评估了右腿肿胀以及踝部区域的exc裂和血红蛋白分泌。自出生以来,该孩子患有右脚踝血管瘤。随后,病变沿腿部逐渐扩散至臀部,该患者患有Klippel-Trenaunay-Weber综合征并伴有腿部继发性纤维素瘤。血管瘤常见于婴儿期,通常是良性的。 Klippel-Trenaunay-Weber综合征的特征是患处毛细血管和静脉畸形,静脉静脉曲张和软组织增生三联征。当该三联征伴有动静脉瘘时,可诊断出帕克斯韦伯综合征。

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